Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:70801027-70801189 | Rare:61 | ||||
chr16:71230674-71230828 | Rare:44 | ||||
chr16:71289187-71289502 | Common:2; Rare:84 | ||||
chr16:71358658-71358772 | Rare:45 | ||||
chr16:71526206-71526472 | Common:1; Rare:41 | ||||
chr16:71564926-71565026 | Rare:33 | ||||
chr16:71626106-71626226 | Common:1; Rare:39 | ||||
chr16:71808924-71809368 | Common:3; Rare:146 | ||||
chr16:71845890-71846017 | Common:2; Rare:41 | ||||
chr16:71884136-71884405 | Common:1; Rare:95 | ||||
chr16:71894214-71894471 | Rare:74 | ||||
chr16:71895244-71895593 | Common:3; Rare:136 | ||||
chr16:72008474-72008847 | Common:6; Rare:159; Clinvar (benign):2 | ||||
chr16:72093451-72093978 | Common:1; Rare:130 | ||||
chr16:74296697-74296944 | Rare:101 |